Year |
Citation |
Score |
2016 |
Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, Macdonald RL. Correction: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. Plos One. 11: e0167264. PMID 27870904 DOI: 10.1371/journal.pone.0167264 |
0.458 |
|
2016 |
Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, Macdonald RL. Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. Plos One. 11: e0162883. PMID 27622563 DOI: 10.1371/Journal.Pone.0162883 |
0.598 |
|
2016 |
Botzolakis EJ, Gurba KN, Lagrange AH, Feng HJ, Stanic AK, Hu N, Macdonald RL. Comparison of GABA-A Receptor αβγ and αβδ Expression Using Flow Cytometry and Electrophysiology: Evidence for Alternate Subunit Stoichiometries and Arrangements. The Journal of Biological Chemistry. PMID 27493204 DOI: 10.1074/Jbc.M115.698860 |
0.633 |
|
2014 |
Todd E, Gurba KN, Botzolakis EJ, Stanic AK, Macdonald RL. GABAA receptor biogenesis is impaired by the γ2 subunit febrile seizure-associated mutation, GABRG2(R177G). Neurobiology of Disease. 69: 215-24. PMID 24874541 DOI: 10.1016/j.nbd.2014.05.013 |
0.666 |
|
2014 |
Lo WY, Lagrange AH, Hernandez CC, Gurba KN, Macdonald RL. Co-expression of γ2 subunits hinders processing of N-linked glycans attached to the N104 glycosylation sites of GABAA receptor β2 subunits. Neurochemical Research. 39: 1088-103. PMID 24213971 DOI: 10.1007/S11064-013-1187-9 |
0.628 |
|
2013 |
Hernandez CC, Gurba KN, Hu N, Macdonald RL. GAbAA Receptor Subunit Rare Variants Identified in Patients with Idiopathic Generalized Epilepsy Alter Receptor Gating and Assembly Biophysical Journal. 104: 275a. DOI: 10.1016/J.Bpj.2012.11.1541 |
0.634 |
|
2012 |
Gurba KN, Hernandez CC, Hu N, Macdonald RL. GABRB3 mutation, G32R, associated with childhood absence epilepsy alters α1β3γ2L γ-aminobutyric acid type A (GABAA) receptor expression and channel gating. The Journal of Biological Chemistry. 287: 12083-97. PMID 22303015 DOI: 10.1074/Jbc.M111.332528 |
0.658 |
|
2012 |
Hernandez CC, Gurba KN, Hu N, Macdonald RL. Mapping GABAA Receptor Single Nucleotide Polymorphisms (SNPs) Linked to Epilepsy: Insights into the Receptor Gating and Assembly Biophysical Journal. 102: 111a. DOI: 10.1016/J.Bpj.2011.11.624 |
0.673 |
|
2011 |
Hernandez CC, Gurba KN, Hu N, Macdonald RL. The GABRA6 mutation, R46W, associated with childhood absence epilepsy, alters 6β22 and 6β2 GABA(A) receptor channel gating and expression. The Journal of Physiology. 589: 5857-78. PMID 21930603 DOI: 10.1113/Jphysiol.2011.218883 |
0.637 |
|
2011 |
Botzolakis EJ, Zhao J, Gurba KN, Macdonald RL, Hedera P. The effect of HSP-causing mutations in SPG3A and NIPA1 on the assembly, trafficking, and interaction between atlastin-1 and NIPA1. Molecular and Cellular Neurosciences. 46: 122-35. PMID 20816793 DOI: 10.1016/j.mcn.2010.08.012 |
0.612 |
|
2011 |
Hernandez CC, Gurba KN, Hu N, Macdonald RL. A novel Polymorphism Linked to Epilepsy Encoding a Missense Mutation in the Pre-M1 Region of a6 Subunits Alters the Gating, but not Trafficking, of GABAa Receptors Biophysical Journal. 100: 271a-272a. DOI: 10.1016/J.Bpj.2010.12.1692 |
0.661 |
|
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